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The ER Stress/UPR axis in chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis


Aghaei, M and Dastghaib, S and Aftabi, S and Aghanoori, M-R and Alizadeh, J and Mokarram, P and Mehrbod, P and Ashrafizadeh, M and Zarrabi, A and McAlinden, KD and Eapen, MS and Sohal, SS and Sharma, P and Zeki, AA and Ghavami, S, The ER Stress/UPR axis in chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis, Life, 11, (1) pp. 1-27. ISSN 2075-1729 (2021) [Refereed Article]


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Copyright 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( licenses/by/4.0/).

DOI: doi:10.3390/life11010001


Cellular protein homeostasis in the lungs is constantly disrupted by recurrent exposure to various external and internal stressors, which may cause considerable protein secretion pressure on the endoplasmic reticulum (ER), resulting in the survival and differentiation of these cell types to meet the increased functional demands. Cells are able to induce a highly conserved adaptive mechanism, known as the unfolded protein response (UPR), to manage such stresses. UPR dysregulation and ER stress are involved in numerous human illnesses, such as metabolic syndrome, fibrotic diseases, and neurodegeneration, and cancer. Therefore, effective and specific compounds targeting the UPR pathway are being considered as potential therapies. This review focuses on the impact of both external and internal stressors on the ER in idiopathic pulmonary fibrosis (IPF) and chronic obstructive pulmonary disease (COPD) and discusses the role of the UPR signaling pathway activation in the control of cellular damage and specifically highlights the potential involvement of non-coding RNAs in COPD. Summaries of pathogenic mechanisms associated with the ER stress/UPR axis contributing to IPF and COPD, and promising pharmacological intervention strategies, are also presented.

Item Details

Item Type:Refereed Article
Keywords:IPF, COPD, epithelium, fibrosis, EndMT, EMT, cancer, ICS, inflammation
Research Division:Biomedical and Clinical Sciences
Research Group:Cardiovascular medicine and haematology
Research Field:Cardiology (incl. cardiovascular diseases)
Objective Division:Health
Objective Group:Clinical health
Objective Field:Diagnosis of human diseases and conditions
UTAS Author:McAlinden, KD (Mr Kielan McAlinden)
UTAS Author:Eapen, MS (Dr Mathew Eapen)
UTAS Author:Sohal, SS (Dr Sukhwinder Sohal)
UTAS Author:Sharma, P (Dr Pawan Sharma)
ID Code:142281
Year Published:2021
Web of Science® Times Cited:9
Deposited By:Health Sciences
Deposited On:2021-01-05
Last Modified:2022-08-25
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